| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2027605 | 1.000 | 0.120 | 21 | 29354452 | intron variant | A/G | snv | 0.48 | 3 | ||
| rs1153280 | 1.000 | 0.120 | 21 | 29305751 | intron variant | G/A | snv | 0.52 | 2 | ||
| rs1153287 | 1.000 | 0.120 | 21 | 29313290 | intron variant | G/A;T | snv | 1 | |||
| rs1153294 | 1.000 | 0.120 | 21 | 29328775 | intron variant | T/C;G | snv | 1 | |||
| rs117214 | 1.000 | 0.120 | 21 | 29348513 | intron variant | C/T | snv | 0.45 | 1 | ||
| rs1447826 | 1.000 | 0.120 | 3 | 74669607 | intergenic variant | T/A;C;G | snv | 1 | |||
| rs1555461176 | 1.000 | 0.120 | 16 | 23634893 | stop gained | -/T | delins | 1 | |||
| rs1975920 | 1.000 | 0.120 | 12 | 27583053 | intron variant | G/T | snv | 0.40 | 1 | ||
| rs2035565 | 1.000 | 0.120 | 2 | 67392524 | intron variant | C/T | snv | 0.74 | 1 | ||
| rs2172905 | 1.000 | 0.120 | 6 | 170019278 | regulatory region variant | C/T | snv | 0.30 | 1 | ||
| rs2832290 | 1.000 | 0.120 | 21 | 29356542 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs2903018 | 1.000 | 0.120 | 19 | 29164379 | intergenic variant | G/A;T | snv | 1 | |||
| rs7015626 | 1.000 | 0.120 | 8 | 124864572 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs7106914 | 1.000 | 0.120 | 11 | 9956424 | intron variant | T/C | snv | 0.38 | 1 | ||
| rs1049074086 | 0.925 | 0.120 | 11 | 1759567 | missense variant | A/G | snv | 7.0E-06 | 9 | ||
| rs199976573 | 0.925 | 0.120 | 4 | 88132618 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 4 | |
| rs78303930 | 0.925 | 0.120 | 1 | 156670593 | missense variant | C/A;G | snv | 4.0E-06; 2.4E-03 | 4 | ||
| rs11644322 | 0.925 | 0.120 | 16 | 79005703 | intron variant | C/T | snv | 0.22 | 3 | ||
| rs1209809979 | 0.925 | 0.120 | 1 | 45568989 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs1370041903 | 0.925 | 0.120 | 6 | 161350185 | stop gained | G/A | snv | 3 | |||
| rs150495372 | 0.925 | 0.120 | 4 | 99313834 | missense variant | C/T | snv | 3.7E-04 | 3 | ||
| rs1537373 | 0.925 | 0.120 | 9 | 22103342 | intron variant | T/G | snv | 0.63 | 3 | ||
| rs2001389 | 0.925 | 0.120 | 10 | 102615501 | intron variant | G/A;C | snv | 3 | |||
| rs2235108 | 0.925 | 0.120 | 8 | 125436547 | 3 prime UTR variant | G/A | snv | 0.25 | 3 | ||
| rs2980879 | 0.925 | 0.120 | 8 | 125469233 | intron variant | A/T | snv | 0.69 | 3 |